homeostasis/metabolism
• mice show increased vulnerability to ischemic stroke, developing an earlier onset of anoxic depolarization and more frequent peri-infarct depolarizations after filament occlusion of the middle cerebral artery associated with rapid expansion of infarct core on diffusion-weighted magnetic resonance imaging and larger perfusion defects on laser speckle flowmetry
• mutants develop larger areas of cerebral blood flow deficit during distal middle cerebral artery occlusion due to increased susceptibility to ischemic depolarizations
• mutant cortical tissue requires a higher cerebral blood flow threshold level for survival compared to wild-type mice
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• transient filament occlusion of the middle cerebral artery for 1 hour produces larger infarcts than in wild-type mice, with more severe cortical, hippocampal, and thalamic involvement
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mortality/aging
• mortality rate following filament occlusion of the middle cerebral artery is higher in mutants, reaching 100% within 24 hours after stroke onset
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nervous system
• mice show increased vulnerability to ischemic stroke, developing an earlier onset of anoxic depolarization and more frequent peri-infarct depolarizations after filament occlusion of the middle cerebral artery associated with rapid expansion of infarct core on diffusion-weighted magnetic resonance imaging and larger perfusion defects on laser speckle flowmetry
• mutants develop larger areas of cerebral blood flow deficit during distal middle cerebral artery occlusion due to increased susceptibility to ischemic depolarizations
• mutant cortical tissue requires a higher cerebral blood flow threshold level for survival compared to wild-type mice
|
• transient filament occlusion of the middle cerebral artery for 1 hour produces larger infarcts than in wild-type mice, with more severe cortical, hippocampal, and thalamic involvement
|
Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
familial hemiplegic migraine | DOID:0060178 | J:193793 |